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1.
Plant Sci ; 185-186: 227-37, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22325885

RESUMO

Corynespora Leaf Fall (CLF) is a major disease of rubber tree (Hevea brasiliensis) caused by the Ascomycota Corynespora cassiicola. Here we describe the cloning and characterization of a gene encoding cassiicolin (Cas), a glycosylated cystein-rich small secreted protein (SSP) identified as a potential CLF disease effector in rubber tree. Three isolates with contrasted levels of aggressiveness were analyzed comparatively. The cassiicolin gene was detected - and the toxin successfully purified - from the isolates with high and medium aggressiveness (CCP and CCAM3 respectively) but not from the isolate with the lowest aggressiveness (CCAM1), suggesting the existence of a different disease effector in the later. CCP and CCAM3 carried strictly identical cassiicolin genes and produced toxins of identical mass, as evidence by mass spectrometry analysis, thus suggesting conserved post-translational modifications in addition to sequence identity. The differences in aggressiveness between CCP and CCAM3 may be attributed to differences in cassiicolin transcript levels rather than qualitative variations in cassiicolin structure. Cassiicolin may play an important role in the early phase of infection since a peak of cassiicolin transcripts occurred in 1 or 2 days after inoculation (before the occurrence of the first symptoms), in both the tolerant and the susceptible cultivars.


Assuntos
Ascomicetos/genética , Proteínas Fúngicas/isolamento & purificação , Regulação Fúngica da Expressão Gênica/genética , Hevea/microbiologia , Micotoxinas/isolamento & purificação , Doenças das Plantas/microbiologia , Sequência de Aminoácidos , Ascomicetos/isolamento & purificação , Ascomicetos/patogenicidade , Sequência de Bases , Clonagem Molecular , Biologia Computacional , DNA Complementar/genética , Proteínas Fúngicas/química , Proteínas Fúngicas/genética , Dados de Sequência Molecular , Micélio/genética , Micélio/isolamento & purificação , Micélio/patogenicidade , Micotoxinas/química , Micotoxinas/genética , Folhas de Planta/microbiologia , RNA Fúngico/genética , RNA Fúngico/metabolismo , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Análise de Sequência de DNA , Virulência
2.
Plant Cell Physiol ; 51(11): 1878-88, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20929914

RESUMO

Quebrachitol is a cyclic polyol and, along with sucrose, is one of the main sugars in Hevea latex. However, in contrast to sucrose, the mechanism and regulation of quebrachitol absorption is still unknown. Screening a latex-derived cDNA library using polyol transporter-specific probes, two full-length cDNAs were isolated, and named HbPLT1 and HbPLT2 (for Hevea brasiliensis polyol transporter 1 and 2, respectively). Their respective sequences exhibited close similarity with the previously cloned acyclic sugar polyol transporters, and shared the main features of the major facilitative superfamily. The functional activity of one of the cDNAs was determined by using an HbPLT2-complemented yeast strain. These strains displayed a marginal absorption of cyclic (inositol) and acyclic (mannitol and sorbitol) polyol but no absorption of sucrose, hexose and glycerol. Active absorption for xylitol was detected, and was competitively inhibited by quebrachitol. HbPLT1 and HbPLT2 expression patterns varied in response to different stimuli. Bark treatment with ethylene resulted in an early and significant up-regulation of HbPLT2 transcripts in laticifers as well as in inner bark cells, when compared with HbPLT1. Other treatments, especially mechanical wounding, strongly induced HbPLT2 transcripts. These data were consistent with the presence of ethylene and a wound-responsive regulatory cis-element on the sequence of the HbPLT2 promoter. All these findings together with those recently obtained for sucrose transporters and aquaporins are discussed in relation to the different roles for quebrachitol in Hevea brasiliensis.


Assuntos
Euphorbiaceae/genética , Proteínas de Plantas/metabolismo , Polímeros/metabolismo , Sequência de Aminoácidos , Transporte Biológico , Clonagem Molecular , DNA Complementar/genética , Genes de Plantas , Hibridização In Situ , Dados de Sequência Molecular , Filogenia , Proteínas de Plantas/classificação , Proteínas de Plantas/genética , Saccharomyces cerevisiae/genética , Homologia de Sequência de Aminoácidos
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